holoprosencephaly 11
holoprosencephaly that has material basis in heterozygous mutation in the CDON gene on chromosome 11q24
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holoprosencephaly 11
Summary
holoprosencephaly 11 is a rare disease[1].
Key Facts
- holoprosencephaly 11's instance of is recorded as rare disease[2].
- holoprosencephaly 11's instance of is recorded as class of disease[3].
- holoprosencephaly 11's subclass of is recorded as holoprosencephaly[4].
- holoprosencephaly 11's subclass of is recorded as genetic disease[5].
- holoprosencephaly 11's subclass of is recorded as autosomal dominant disease[6].
- holoprosencephaly 11's OMIM ID is recorded as 614226[7].
- holoprosencephaly 11's OMIM ID is recorded as 614226[8].
- holoprosencephaly 11's Disease Ontology ID is recorded as DOID:0110877[9].
- holoprosencephaly 11's genetic association is recorded as CDON[10].
- holoprosencephaly 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110877[11].
- holoprosencephaly 11's exact match is recorded as http://identifiers.org/doid/DOID:0110877[12].
- holoprosencephaly 11's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[13].
- holoprosencephaly 11's UMLS CUI is recorded as C3280215[14].
- holoprosencephaly 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- holoprosencephaly 11's Mondo ID is recorded as MONDO_0013642[16].
- holoprosencephaly 11's UniProt disease ID is recorded as DI-03230[17].